SCT is diagnosed with an ultrasound exam.Ī sacrococcygeal teratoma is categorized by its location and severity: An SCT may be suspected if the mother’s blood work shows a high alpha fetoprotein or if a sonogram shows the uterus is larger than it should be. SCTs may grow very large, but are usually not malignant (cancerous). It is more common in female than male babies. It is the most common tumor found in newborns though it only occurs in about one in 35,000 births. “We are humbled and thankful because we received a gift that not everyone is lucky enough to get.”Ī sacrococcygeal teratoma (SCT) is rare tumor located at the base of the coccyx, or tailbone. “We turned to Texas Children’s because we wanted that hope that they would be able to help her,” recalls Keri. ![]() Today, Macie is a thriving, playful 9-year-old, and remains every bit the miracle girl she was before her birth. ![]() “There’s no evidence, apart from the scar, that lets you know she’s gone through anything of that nature. “If we didn’t tell people, no one would know,” says Chad. Besides the small scar on her tailbone, Macie shows no signs or indications that she endured such a life-threatening experience. Macie was discharged from Texas Children’s one month later and joined her four siblings at home in Laredo. It was no coincidence that her parents gave her the middle name of Hope. Weighing in at 6 lbs, 1 oz., Macie was a healthy baby girl. Ten weeks after the surgery at 35 weeks, Macie Hope McCartney made her second appearance in the world, this time via C-section. Would the heart respond positively? The answer was a resounding yes, and baby Macie continued to develop safe inside her mother’s womb. Keri was given more than seven times the normal amount of anesthesia to prevent labor and protect the baby.Ī critical test came when the tumor, which filled Olutoye’s hand, was removed. Oluyinka Olutoye opened Keri’s womb, partially removed her 25-week-old daughter, and cut away most of the tumor in a single 4-hour procedure. On February 28, 2008, a surgical team led by Dr. “We talked to the doctors and knew that if things didn’t work out that we’d fought for her and done everything we could.” “It brought me such comfort during that time that as sick as she was, a 25-week baby, that they saw her life worth fighting for,” says Keri. The surgery was scheduled for the next day. With Macie’s heart failing, the McCartney’s had one day to make a decision and they decided they couldn’t say no to their baby. “If there was any place this could happen, Texas Children’s was the place.” “For the first time, we at least knew that good or bad the outcome, we were in a place where they would walk us through the whole thing,” says Chad. A team of nearly 30 specialists met to evaluate the McCartney baby’s case and came to a unanimous decision.ĭespite the fact that few operations of its kind had ever been performed or even been successful, fetal surgery offered the McCartney’s the potential for a better outcome. and Texas Children’s Fetal Center responded. The McCartney’s OB/GYN searched for help across the U.S. ![]() “Our OB/GYN explained that our baby’s odds of survival were less than 10% because the tumor was so blood-filled,” recalls Keri. This type of very rare tumor, found in only 1 of 35,000 pregnancies, was drawing on her blood supply and would ultimately lead to heart failure. The ultrasound revealed a grapefruit-sized mass, called a sacrococcygeal teratoma (SCT), growing out of the baby’s tailbone. But that excitement quickly turned to fear when the image on the screen caused the technician to fall silent. Nine years ago, at their 20-week ultrasound check, Keri and Chad McCartney were thrilled to learn their fifth and final child would be a girl.
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